100 Clinical Research Acronyms

If you’re just starting your career in Clinical Research, trying to understand all of the acronyms used in various roles can be confusing. To help, we’ve put together this list of 100 acronyms used in Clinical Research for you to know ...

Related Keywords

, House Clinical Research , Ingredient Application Program Interface , Health Information , Good Laboratory Practice , Clinical Research Coordinator , Contract Safety Organisation , Clinical Research , Ethics Committee , Clinical Development Plan , Research Ethics Committee , Academic Research Organisation , Trial Management Organisation , Competent Authority , Clinical Research Management System , Drug Administration , Data Monitoring Committee , Clinical Research Organisation Contract , Clinical Trials Reporting Program , Clinical Trials Office , Contract Manufacturing Organisation , Scientific Review Committee , Electronic Health Record , Alcoa , Pharmiweb Jobs , Adverse Drug , Active Pharmaceutical Ingredient , Application Program , Academic Research , Biological Licensing , Centralised Clinical Trials Office , Clinical Trials , Clinical Data , Clinical Data Management , Clinical Development , Clinical Data Update , Contract Manufacturing , Clinical Project , Case Report , Clinical Research Management , Clinical Research Organisation , Contract Research , Clinical Study , Contract Safety , Clinical Trial Authorisation , Common Terminology Criteria , Clinical Trial Management , Clinical Trials Reporting , Data Monitoring , Data Management , Data Safety Monitoring , Electronic Clinical Outcome , Electronic Case Report , Electronic Data , Electronic Health , Electronic Medical , Electronic Patient Reported , Electronic Trial Master , Good Clinical , Good Documentation , General Data Protection , Good Laboratory , Good Manufacturing , Good Pharmacovigilance , Informed Consent , Investigational Device , Independent Ethics , Investigational Medical , Investigational Medicinal Product Dossier , Investigational New Drug Application , Institutional Review , Long Term Follow , Marketing Authorisation Application , Multiple Ascending , Medical Record , New Drug Application , Normal Healthy , Outside Safety , Protected Health , Protocol Review , Qualifying Clinical , Quality Management , Research Ethics , Single Ascending , Serious Adverse , Statistical Analysis , Source Document , Site Investigator , Standard Operating , Scientific Review , Suspected Unexpected Serious Adverse , Trial Master , Trial Management , Unanticipated Adverse Device , Unexpected Adverse Drug ,